# Han Feng, Inc., Greensboro, NC – FDA Inspections

Source: https://www.keypedia.com/companies/han-feng-inc/af703247-3eec-4708-8d25-3dd3543c91c1

> Inspection records and compliance data for Han Feng, Inc. in Greensboro, North Carolina. 6 FDA inspections on record, last inspected May 14, 2026.

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## Details

- Name: Han Feng, Inc.
- FEI Number: 3010512538
- Address Line 1: 6001a W Market St
- City: Greensboro
- State: North Carolina
- Zip Code: 27409
- Country Name: United States
- Address: 6001a W Market St, Greensboro, North Carolina 27409, United States
- Country: United States

## Related Documents

- FDA Inspection 1318956 - Han Feng, Inc. - 2026-05-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2026
- FDA Inspection 1230280 - Han Feng, Inc. - 2024-02-07 — source: FDA, date: February 7, 2024
- [FDA Inspection 1145962 - Han Feng, Inc. - 2021-07-12](https://www.keypedia.com/records/fda_inspections/han-feng-inc/2fb34df8-66b5-45b5-84da-91bb3bc9fd3d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2021
- FDA Inspection 1039976 - Han Feng, Inc. - 2018-01-10 — source: FDA, date: January 10, 2018
- FDA Inspection 681163 - Han Feng, Inc. - 2010-09-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2010
- FDA Inspection 681163 - Han Feng, Inc. - 2010-09-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2010
- [FDA Inspection 681163 - Han Feng, Inc. - 2010-09-17](https://www.keypedia.com/records/fda_inspections/han-feng-inc/fa6fcc86-43a2-4dd4-9afb-fd077f712369) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2010
- FDA Inspection 570588 - Han Feng, Inc. - 2009-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2009
- FDA Inspection 570588 - Han Feng, Inc. - 2009-02-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2009
- FDA Inspection 570588 - Han Feng, Inc. - 2009-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2009

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